Product Recalls in New York

Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,911 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
1,911 in last 12 months

Showing 3548135500 of 55,896 recalls

Medical DeviceNovember 12, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 728321 Computed Tomography X-ray systems intended to produce...

The Issue: Software error due to the filament on timer

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 728323 Recalled by Philips Medical Systems (Cleveland)...

The Issue: Software error due to the filament on timer

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 728232 Computed Tomography X-ray systems intended to produce...

The Issue: Software error due to the filament on timer

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodNovember 11, 2016· House Of Flavors, Inc.

Recalled Item: Ashby's Sterling Peanut Butter Landslide Ice Cream Recalled by House Of...

The Issue: House of Flavors, Inc. is voluntarily recalling a limited portion of Ashby's...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 11, 2016· First Source, LLC

Recalled Item: Wegmans Milk Chocolate Covered Pretzels Recalled by First Source, LLC Due to...

The Issue: Milk Chocolate covered pretzels have incorrect rear label. The rear label is...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 11, 2016· Greatbatch Medical

Recalled Item: ViaPeel PTFE Peelable Introducer 5FR Recalled by Greatbatch Medical Due to...

The Issue: Greatbatch received complaints with the ViaPeel Introducer Sheath 5FR, of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2016· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...

The Issue: Lack of 510k clearance for design modification.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2016· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...

The Issue: Lack of 510k clearance for design modification.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2016· Stryker Sustainability Solutions

Recalled Item: Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed...

The Issue: An increase in reports indicating that the reprocessed H12LP Trocar...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2016· Medtronic Inc

Recalled Item: ev3 Recalled by Medtronic Inc Due to Medtronic identified an issue with...

The Issue: Medtronic identified an issue with specific models and lots of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugNovember 9, 2016· VistaPharm, Inc.

Recalled Item: Lactulose Solution Recalled by VistaPharm, Inc. Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: bulk solution tested...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2016· Sandoz Inc

Recalled Item: L-Cysteine Hydrochloride Injection Recalled by Sandoz Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2016· Sandoz Inc

Recalled Item: L-Cysteine Hydrochloride Injection Recalled by Sandoz Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 9, 2016· Fabi-saa Inc.

Recalled Item: Fabi-saa Melcochas Candy Net Wt. 8 oz. Fabi-Saa Inc. 39 Recalled by Fabi-saa...

The Issue: NYSDAM analysis revealed the presence of yellow #5 in Melcochas Candy.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 9, 2016· Seth Ellis Chocolatier, LLC

Recalled Item: Free2b Sun Cups Chocolate. Made With SunButter Sunflower Spread. Packaged...

The Issue: Free2b Foods recalled the Sun Cups Chocolate due to potential contamination...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 9, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: GAM Kirschner Wire Recalled by Stryker Howmedica Osteonics Corp. Due to A...

The Issue: A review of packaging revealed the seal integrity of the pouch may be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2016· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 4.0 Recalled by RAYSEARCH LABORATORIES AB Due to Software...

The Issue: Software anomaly; an issue was found with the proton Pencil Beam Scanning...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Virtual XD Test Pack Heavy/Light Fast Set Recalled by Ivoclar Vivadent, Inc....

The Issue: The firm received complaints claiming the dental material failed to set up....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2016· Elana, Inc.

Recalled Item: Elana Surgical KitHUD The Elana Surgical KitHUD Recalled by Elana, Inc. Due...

The Issue: Elana has issued this Field Action to voluntarily remove specific serial...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2016· Halyard Health, Inc

Recalled Item: Halyard C-Section Drape with Clear Screen and Full Incise (Non-Sterile)...

The Issue: Drapes within the affected lots may include a manufacturing variation that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing